Noninvasive prenatal fetal aneuploidy and microdeletion panel:-:Pt:WBC.DNA Plas.cfDNA:-:Dosage
of chromosome specific cf DNA - CISMeF
Noninvasive prenatal fetal aneuploidy and microdeletion panel:-:Pt:WBC.DNA Plas.cfDNA:-:Dosage
of chromosome specific cf DNALOINC code
Preferred Label : Noninvasive prenatal fetal aneuploidy and microdeletion panel:-:Pt:WBC.DNA Plas.cfDNA:-:Dosage
of chromosome specific cf DNA;
LOINC status : ACTIVE;
LOINC display name : Noninvasive prenatal fetal aneuploidy and microdel panel Dosage of chromosome-specific
cfDNA (Plasma cell-free WBC DNA);
LOINC long common name : Noninvasive prenatal fetal aneuploidy and microdeletion panel based on Plasma cell-free
WBC DNA by Dosage of chromosome-specific circulating cell free (ccf) DNA;
LOINC short name : NIP aneu microdel pnl WBC.DNA cfDNA;
LOINC description : Noninvasive prenatal screening is used to assess fetal risk for various genetic conditions
without requiring invasive maternal procedures such as amniocentesis or chorionic
villus sampling. Cell-free DNA (cfDNA) in maternal plasma comes from both fetal and
maternal sources, and depending on the technology used, this DNA can be used to determine
fetal risk for a variety of conditions including aneuploidy (e.g., Trisomy 21, Monosomy
X) and microdeletions (e.g., 22q11.2 deletion). This panel was developed for, but
is not limited in use to, Natera's Panorama prenatal test, which incorporates SNP
analysis of maternal white blood cell DNA with combined maternal and fetal cfDNA SNP
analysis. Natera's proprietary informatics analysis method (NATUS) effectively subtracts
the maternal genotype from the cfDNA genotype and analyzes the remaining fetal cfDNA
genotype for certain aneuploidies and microdeletion syndromes.;